Team:DTU-Denmark/Experiments

From 2013.igem.org

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(Verification of Transformants)
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In order to verify and characterize our Mutant 1 (aerobic, Ammonia -> Nitrite) and Mutant 2 (anaerobic, Nitrite -> Nitrous Oxide) transformants, we performed the following experiments.
In order to verify and characterize our Mutant 1 (aerobic, Ammonia -> Nitrite) and Mutant 2 (anaerobic, Nitrite -> Nitrous Oxide) transformants, we performed the following experiments.
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=== Anaerobic production of nitrous oxide from nitrite ===
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=== Mutant1: Aerobic consumption of ammonium and hydroxylamine ===
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Grow our transformed Mutant 2 anaerobically in the presence of varying concentrations of nitrite; measure the amount of nitrous oxide producedControls are untransformed ''E. coli'' and ''P. aeruginosa''The results from this experiment are complicated by the fact that measurements of nitrous oxide are extremely sensitive and the sensors did not always give reliable data.
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Grow AMO and HAO transformants aerobically in the presence of ammonia and hydroxylamine respectivelyWe found that the AMO transformant used ammonia more quickly than a nontransformed ''E. coli'' controlWe also found that hydroxylamine was toxic to the cells, and did not detect nitrite production in our HAO transformant.  
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[[Team:DTU-Denmark/Experiment2|Experiment details -- Anaerobic production of nitrous oxide from nitrite]]
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[[Team:DTU-Denmark/Experiment4|Experiment details -- Aerobic consumption of ammonium and hydroxylamine]]
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=== Aerobic consumption of ammonium and hydroxylamine ===
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=== Mutant 2: Anaerobic production of nitrous oxide from nitrite ===
-
Grow AMO and HAO transformants aerobically in the presence of ammonia and hydroxylamine respectivelyWe found that the AMO transformant used ammonia more quickly than a nontransformed ''E. coli'' controlWe also found that hydroxylamine was toxic to the cells, and did not detect nitrite production in our HAO transformant.  
+
Grow our transformed Mutant 2 anaerobically in the presence of varying concentrations of nitrite; measure the amount of nitrous oxide producedControls are untransformed ''E. coli'' and ''P. aeruginosa''The results from this experiment are complicated by the fact that measurements of nitrous oxide are extremely sensitive and the sensors did not always give reliable data.
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[[Team:DTU-Denmark/Experiment4|Experiment details -- Aerobic consumption of ammonium and hydroxylamine]]
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[[Team:DTU-Denmark/Experiment2|Experiment details -- Anaerobic production of nitrous oxide from nitrite]]
== Bioreactor ==
== Bioreactor ==

Revision as of 21:32, 29 September 2013

Experiments

Contents

Initial Characterization of E. coli

Initially, we did two experiments to characterize untransformed E. coli under conditions that would be present during wastewater treatment.

Toxicity of Nitrite, Nitrate and Ammonium to E. coli

The purpose of this experiment was to determine whether the ions nitrite, nitrate and ammonium are toxic to E. coli, and at what concentration. We used the BioLector to grow an E. coli strain that constitutively expresses RFP in the presence of these ions (at a range of concentrations), and measure the OD and fluorescence of the cells as a proxy for growth. We found that at high concentrations ammonium (>=500mM) and nitrate (>=25mM) were toxic to E. coli. However, these concentrations are much higher than we would expect to find in wastewater, so we do not expect these ions to be toxic to our cells under normal operating conditions.

Experiment details -- Toxicity of Nitrite, Nitrate and Ammonium to E. coli

Nitrite stability in anaerobic E. coli

To measure how much nitrite would be consumed by competing pathways in Mutant 2, we grew untransformed E. coli anaerobically in the presence of varying concentrations of nitrite and measured the amount of ammonia and nitrite present. We found that a pathway to convert nitrite to ammonium is active, and therefore our Nir pathway will need to outcompete this pathway.

Experiment details -- Nitrite stability in anaerobic E. coli

Verification of Transformants

In order to verify and characterize our Mutant 1 (aerobic, Ammonia -> Nitrite) and Mutant 2 (anaerobic, Nitrite -> Nitrous Oxide) transformants, we performed the following experiments.

Mutant1: Aerobic consumption of ammonium and hydroxylamine

Grow AMO and HAO transformants aerobically in the presence of ammonia and hydroxylamine respectively. We found that the AMO transformant used ammonia more quickly than a nontransformed E. coli control. We also found that hydroxylamine was toxic to the cells, and did not detect nitrite production in our HAO transformant.

Experiment details -- Aerobic consumption of ammonium and hydroxylamine

Mutant 2: Anaerobic production of nitrous oxide from nitrite

Grow our transformed Mutant 2 anaerobically in the presence of varying concentrations of nitrite; measure the amount of nitrous oxide produced. Controls are untransformed E. coli and P. aeruginosa. The results from this experiment are complicated by the fact that measurements of nitrous oxide are extremely sensitive and the sensors did not always give reliable data.

Experiment details -- Anaerobic production of nitrous oxide from nitrite

Bioreactor

Finally, in order to see if the long term behaviour of our Nir transformant, we grew it in a bioreactor.

Experiment details -- Growth of Nir transformant in Bioreactor